Label: VERAPAMIL HYDROCHLORIDE- verapamil hydrochloride tablet, extended release
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Contains inactivated NDC Code(s)
NDC Code(s): 51655-956-52 - Packager: Northwind Pharmaceuticals
- This is a repackaged label.
- Source NDC Code(s): 68462-260
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 27, 2014
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PRINCIPAL DISPLAY PANEL
NDC: 51655-956-52
MFG: 68462-260-05
Verapamil Hydrohloride ER 240 MG
30 tablets
RX only
Lot#: NW08220001
Exp. Date: 02/2016
Each extended release tablet film-coated tablet contains verapamil hydrochloride USP 240mg.
Dosage: See package insert
Store at 68 to 77 degrees F. Protect from light and moisture.
Store in a tight, light-resistant container (See USP). Keep out of the reach of children.
Mfg by: Glenmark Generics Ltd India for Glenmark Generics Inc, NJ USA Lot# 02140734
Repackaged by: Northwind Pharmaceuticals, Indianapolis, IN 46256
- WARNINGS AND PRECAUTIONS
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INGREDIENTS AND APPEARANCE
VERAPAMIL HYDROCHLORIDE
verapamil hydrochloride tablet, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-956(NDC:68462-260) Route of Administration oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE 240 mg in 30 Product Characteristics Color brown Score no score Shape OVAL Size 19mm Flavor Imprint Code G74 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51655-956-52 30 in 1 BOTTLE, DISPENSING Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078906 05/27/2014 Labeler - Northwind Pharmaceuticals (036986393) Registrant - Northwind Pharmaceuticals (036986393) Establishment Name Address ID/FEI Business Operations Northwind Pharmaceuticals 036986393 repack(51655-956)